Effects and mechanisms of total glucosides of paeony on synoviocytes activities in rat collagen-induced arthritis

被引:79
作者
Chang, Yan [1 ]
Wei, Wei [1 ]
Zhang, Lei [1 ]
Xu, Hong-Mei [2 ]
机构
[1] Anhui Med Univ, Inst Clin Pharmacol, Key Lab Antiinflammatory & Immunopharmacol Anhui, Key Lab Res & Dev Chinese Med Anhui Prov, Hefei 230032, Anhui, Peoples R China
[2] Hefei Univ Technol, Hefei 230009, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Collagen-induced arthritis; Synoviocytes; Total glucosides of paeony; Cyclic adenosine monophosphate; Prostaglandin E-2; E-prostanoid; NECROSIS-FACTOR-ALPHA; PROSTAGLANDIN E-2 RECEPTORS; AIRWAY SMOOTH-MUSCLE; MODULATE TNF-ALPHA; RHEUMATOID-ARTHRITIS; ADJUVANT ARTHRITIS; SYNOVIAL FIBROBLASTS; UP-REGULATION; PERITONEAL-MACROPHAGES; PROSTANOID RECEPTORS;
D O I
10.1016/j.jep.2008.09.028
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The aim of the Study was to investigate the effects of TGP, an active compound extracted from the roots of Paeonia lactiflora Pall, on the activities of synoviocytes in rats with collageninduced arthritis (CIA) and its possible mechanisms. CIA was induced in male Sprague-Dawley (SD) rats immunized with chicken type II collagen (CII) in Freund's complete adjuvant (FCA). Synoviocytes proliferation was determined by 3-(4,5-2dimethylthiazal-2yl) 2,5-diphenyltetrazoliumbromide (MTT) assay. Tumor necrosis factor alpha (TNF-alpha), interleukin-1 (IL-1), prostaglandin E-2 (PGE(2)) and cyclic adenosine monophosphate (cAMP) levels in synoviocytes were measured by radioimmunoassay (RIA). E-prostanoid (EP)(2) and EP4 receptors were analyzed by Western blot analysis. The results showed that TGP significantly inhibited the proliferation of synoviocytes, decreased the production of IL-1, TNF-alpha and PGE(2) and elevated the levels of cAMP Further Study showed that TGP could up-regulate the expression of EP2. and EP4. These results indicated that TGP might exert its anti-inflammatory effects through inhibiting the production of pro-inflammatory mediators in synoviocytes of CIA rats, which might be associated with its ability to regulate cAMP-dependent EP2/EP4-mediated pathway. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:43 / 48
页数:6
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